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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC2946 Kongensin D
Natural anti-TNBC agent, significantly suppressing the triple-negative breast cancer (TNBC) tumor growth without causing side effects
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DCC2945 Kmup-4
Novel enhancer of cGMP activity; Aortic smooth muscle relaxant
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DCC2944 Kmup-3
Novel enhancer of cGMP activity; Aortic smooth muscle relaxant
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DCC2943 Kms88009
Novel inhibitor of amyloid-β aggregation, ameliorating the neurodegenerative disorder
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DCC2942 kms80013
Novel inhibitor of amyloid-
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DCC2941 Kmn-80
Novel Potent and Selective EP4 Agonist
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DCC2940 Kmn-010034
Novel Potent Hematopoietic Prostaglandin D2 Synthase (H-PGDS) Inhibitor
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DCC2939 kmi-1764
Novel BACE1 inhibitor with a non-acidic heterocycle at the P1' position
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DCC2938 Km-5-66
Novel inhibitor of the BfrB-Bfd complex, binding BfrB in the P. aeruginosa cytosol, blocking the BfrB-Bfd interaction and inhibiting iron mobilization from BfrB, resulting in cytosolic iron limitation that is manifested in a pyoverdine hyperproduction phe
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DCC2937 Km-5-25
Novel inhibitor of the BfrB-Bfd complex, binding BfrB in the P. aeruginosa cytosol, blocking the BfrB-Bfd interaction and inhibiting iron mobilization from BfrB, resulting in cytosolic iron limitation that is manifested in a pyoverdine hyperproduction phe
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DCC2936 km10340
Selective S1P3 agonist
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DCC2935 Km05382
CDK9 inhibitor, inhibiting transcription of GAPDH
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DCC2934 Boc-phe-leu-glup(oph)
DCC2933 Kl-l9p
Novel antibiotic sensitizer, promoting the rearrangement of the bacterial membrane that enables hydrophobic antibiotics to permeate, strongly sensitizing Gram-negative bacteria to linezolid (Lzd), rifampicin (Rif), or clarithromycin (Clr)
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DCC2932 Klk6-in-42
First-in-class inhibitor of Kallikrein-related peptidase 6 (KLK6), promoting the differentiation of OPCs into mature oligodendrocytes in vitro
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DCC2931 Klk6-in-32
First-in-class inhibitor of Kallikrein-related peptidase 6 (KLK6), promoting the differentiation of OPCs into mature oligodendrocytes in vitro
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DCC2930 Klebsazolicin
Novel inhibitor of 70S ribosome by obstructing the peptide exit tunnel
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DCC2929 Kld-12
Self-assembling peptide, forming a hydrogel matrix to support growth of cells in the presence of an ionic solution, enhancing chondrogenic differentiation of bone marrow stromal cells (BMSCs)
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DCC2928 Kl-1156
Novel NF-κB inhibitor and lipopolysaccharide (LPS)-induced nitric oxide production inhibitor
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DCC2927 Kkha-761
Potent D3 receptor antagonist with high 5-HT1A receptor affinity
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DCC2926 Kj-pyr-10
Novel specific inhibitor of MYC
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DCC2925 Kjm429
Novel TRPV1 antagonist
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DCC2924 Kist301080
Novel ROS1 kinase inhibitor
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DCC2923 Kist301072
Novel ROS1 kinase inhibitor
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DCC2922 Kir1.1-in-a
Novel potent and selective inhibitor of kir1.1 channels
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DCC2921 kin100
Novel inducer of the ISG54 promoter, causing IRF-3 translocation
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DCC2920 Ki-ms2-008
Novel Max-binding modulator, attenuating Myc-driven transcription and stabilizing the Max homodimer
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DCC2919 Kif18a Inhibitor 23
Novel KIF18A inhibitor, causing significant mitotic arrest in vivo, binding at the interface of KIF18A and tubulin
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DCC2918 Ki23057
Novel FGFR2 inhibitor, enhancing the chemosensitivity of drug-resistant gastric cancer cell lines
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DCC2917 Khg26693
Novel anti-inflammatory and antioxidant agent, significantly decreasing blood glucose, triglycerides, and cholesterol and increased insulin
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